The nuclear gene TAT encodes the mitochondrial protein Tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.
The nuclear gene TAT encodes the mitochondrial protein Tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.
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Safety & Storage
Storage Temperature
After reconstitution, the TAT antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
Amino acids 169-208 (FSLYKTLAESMGIEVKLYNLLPEKSWEIDLKQLEYLIDEK-human) were used as the immunogen for the TAT antibody.
STORAGE BUFFER
0.5mg/ml if reconstituted with 0.2ml sterile DI water
APPLICATION DETAILS
Western blot: 0.5-1ug/ml
APPLICATION NOTES
Optimal dilution of the TAT antibody should be determined by the researcher.
LOCALIZATION
Cytoplasmic
BUFFER
Lyophilized from 1X PBS with 2.5% BSA and 0.025% sodium azide
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Shipping & Handling
Shipped In
Cold Packs
Safety & Storage
Storage Temperature
After reconstitution, the TAT antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
Safety Statement
This antibody is available for research use only.
Regulatory & Compliance
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